FDA 510(k)

V-SPERM WASH

K-Number: K223117 · 2023-01-31

Decision Date2023-01-31

Product CodeMQL

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

V-SPERM WASH is a medical device manufactured by Vitromed GmbH. It received FDA 510(k) clearance on 2023-01-31 under approval number K223117. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-SPERM WASH?

V-SPERM WASH is a medical device that received FDA 510(k) clearance on 2023-01-31. It is manufactured by Vitromed GmbH. The 510(k) number is K223117.

When was V-SPERM WASH approved by the FDA?

V-SPERM WASH received FDA 510(k) clearance on 2023-01-31, under approval number K223117.

What company makes V-SPERM WASH?

V-SPERM WASH is manufactured by Vitromed GmbH.

What is the FDA product code for V-SPERM WASH?

The FDA product code for V-SPERM WASH is MQL.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.